{
  "id": 23108,
  "label": "familial acanthosis nigricans",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0043003",
  "properties": {
    "xrefs": [
      "MEDGEN:419638",
      "MESH:C531598",
      "OMIM:100600",
      "UMLS:C2930792"
    ],
    "synonyms": [
      "hereditary acanthosis nigricans (disease)",
      "acanthosis nigricans"
    ],
    "categories": [
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      }
    ],
    "definition": "An instance of acanthosis nigricans (disease) that is caused by an inherited modification of the individual's genome."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 8454,
      "label": "acanthosis nigricans",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4496
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3138",
          "EFO:1000660",
          "HP:0000956",
          "ICD10CM:L83",
          "ICD10WHO:L83",
          "MEDGEN:54",
          "MESH:D000052",
          "NCIT:C26687",
          "Orphanet:924",
          "SCTID:402599005",
          "UMLS:C0000889",
          "Wikipedia:Acanthosis_nigricans",
          "icd11.foundation:71488193"
        ],
        "synonyms": [
          "acanthosis nigricans",
          "acanthosis nigricans (disease)",
          "an - acanthosis nigricans"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "A melanotic cutaneous lesion that develops in the axilla and other body folds. It may be idiopathic, drug-induced, or it may be associated with the presence of an endocrine disorder or malignancy."
      },
      "child_count": 2,
      "reference_id": "MONDO:0007035"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6820
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MESH:D012873",
          "SCTID:239001006"
        ],
        "synonyms": [
          "disease, genetic skin",
          "diseases, genetic skin",
          "genetic skin disease",
          "genetic skin diseases",
          "genodermatosis",
          "skin disease, genetic"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "An instance of skin disease that is caused by a modification of the individual's genome."
      },
      "child_count": 228,
      "reference_id": "MONDO:0100118"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 8454,
      "label": "acanthosis nigricans"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder"
    }
  ]
}